FDA Adverse Event
Injury
Summary report: N
ZIMMER MARCHETTI FEMORAL NAIL
MDR report key: 3110920
·
Received May 9, 2013
Report
- Report Number
- 1822565-2013-00772
- Event Type
- Injury
- Date Received
- May 9, 2013
- Report Date
- April 9, 2013
- Manufacturer
- ZIMMER, INC.
- Product Code
- HSB
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IT
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
THE REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.
Description of Event or Problem · 1
IT IS REPORTED THAT THE PT IS EXPERIENCING PAIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 204784 | ZIMMER MARCHETTI FEMORAL NAIL | TRAUMA PROSTHESIS | HSB | ZIMMER, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |